Exercise and Nutritional Rehabilitation in Patients With Cancer (ENeRgy)
Primary Purpose
Cachexia; Cancer, Diet Modification, Physical Activity
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
ProSure
Physical Exercise
Sponsored by
About this trial
This is an interventional supportive care trial for Cachexia; Cancer
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of advanced cancer (defined as metastatic or locally advanced cancer not amenable to curative treatment).
- Outpatient
- ≥18years
- Karnofsky score ≥ 60
- Prognosis greater than 3 months
- Able to complete trial based assessments
- Under care of community services at Marie Curie or St Columba's Hospices
- Ability to comply with trial protocol
- Ability to provide and have capacity to consent
- Agree to attend trial centre for trial related activity (St Columba's Hospice)
Exclusion Criteria:
- Undergoing anti-cancer therapy (hormonal treatment or bisphosphonates permitted)
- Using enteral nutrition (NG or similar) or parenteral nutrition
- Co-enrolment in drug trials
- Inability to swallow
Sites / Locations
- University of Edinburgh
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Rehabilitation
Waiting list Control
Arm Description
Advanced cancer patients will receive an 8 week rehabilitation intervention consisting of physical exercise and nutritional supplementation, along with standard care
Standard care alone for the 8 week trial period, followed by participants being offered the rehabilitation programme
Outcomes
Primary Outcome Measures
Feasibility of Rehabilitation programme
Compliance with treatment and trial procedures
Secondary Outcome Measures
Patient quality of life
Measured by EORTC QLQ-C15-PAL questionnaire
Carer quality of life
Measured by CQOLC questionnaire
Change in physical function
Mean daily step count, measured by Physical Activity Meter over 5 days
Change in physical function
Measured by two-minute walk test (metres/feet covered)
Change in physical function
Measured by Karnofsky performance status (KPS) at baseline, mid and endpoint
Change in physical function
Measured by timed up-and-go test (Seconds)
Change in physical function
Measured by Life Space Assessment scores
Sleep quality
Measured by physical activity meter at baseline and endpoint (Mean sleep hours, mean hours restless and hours awake)
Nutritional status
Height and weight measured at baseline, mid and endpoint assessment (m, Kg and combined as kg/m2)
Nutritional status
Measured by PG-SGA nutritional assessment (PG-SGA point score)
Contamination in the control group
Measured by dietary intake using 24 hour recall (patient diary entries)
Contamination in the control group
Measured by change in measures of physical function (see outcomes 4-8) in control group from baseline measurement to endpoint
Full Information
NCT ID
NCT03316157
First Posted
September 22, 2017
Last Updated
March 10, 2020
Sponsor
University of Edinburgh
Collaborators
Marie Curie Hospice, Belfast, Accord Clinical Research, NHS Lothian
1. Study Identification
Unique Protocol Identification Number
NCT03316157
Brief Title
Exercise and Nutritional Rehabilitation in Patients With Cancer
Acronym
ENeRgy
Official Title
Exercise and Nutritional Rehabilitation in Patients With Cancer, Randomised (1:1) Unblinded Feasibility Trial of a Rehabilitation Programme (Exercise and Nutrition) Versus Waiting List Control, in Patients With Advanced Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
January 30, 2018 (Actual)
Primary Completion Date
April 24, 2019 (Actual)
Study Completion Date
July 3, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Edinburgh
Collaborators
Marie Curie Hospice, Belfast, Accord Clinical Research, NHS Lothian
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In patients with incurable cancer, general deterioration in their ability to walk, exercise and care for themselves is often regarded as an inevitable consequence of this. In 2015, Hospice UK published a report advocating "Rehabilitative Palliative Care".
However there is limited robust evidence on which to base this approach. Reviews of the literature show limited study numbers but do suggest that rehabilitation may be feasible for advanced cancer patients. However key components were not clear and no recommendations could be given.
This trial is designed primarily to test the feasibility of a rehabilitation programme (exercise and nutritional supplementation) in advanced cancer patients. Feasibility will be the primary outcome measure including rates of recruitment and compliance. Secondary outcome measures include impact on physical function, nutritional status, quality of life for patients and their carers. We will also assess the health economic impact by assessing patient health facility use throughout the trial.
40 patients with advanced cancer living in the community will be recruited from two hospice palliative care teams in Edinburgh. These patients will be randomised in to either the treatment arm: the rehabilitation programme plus standard care, or the control arm: standard care alone. The treatment arm will consist of an 8 week rehabilitation programme, supervised at weekly clinics by a physiotherapist and dietician.
To minimise contamination the control group will be offered the treatment at the end of the 8 weeks (waiting list control).
Measurements will be made for both groups and compared at baseline (week 0), midpoint (week 5) and endpoint (week 9). Recommendations for a larger UK wide trial will be made from the findings of this study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cachexia; Cancer, Diet Modification, Physical Activity, Advanced Cancer
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomised (1:1) unblinded feasibility trial of a rehabilitation programme (exercise and nutrition) versus waiting list control, in patients with advanced cancer
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rehabilitation
Arm Type
Experimental
Arm Description
Advanced cancer patients will receive an 8 week rehabilitation intervention consisting of physical exercise and nutritional supplementation, along with standard care
Arm Title
Waiting list Control
Arm Type
No Intervention
Arm Description
Standard care alone for the 8 week trial period, followed by participants being offered the rehabilitation programme
Intervention Type
Dietary Supplement
Intervention Name(s)
ProSure
Intervention Description
Patients will take 2x 220mL nutritional supplements per day for 8 weeks and be given dietary advice to optimise their nutrition
Intervention Type
Behavioral
Intervention Name(s)
Physical Exercise
Intervention Description
Patients will receive an individualised exercise regimen consisting of 60 minutes aerobic and 3x resistance elements per week
Primary Outcome Measure Information:
Title
Feasibility of Rehabilitation programme
Description
Compliance with treatment and trial procedures
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Patient quality of life
Description
Measured by EORTC QLQ-C15-PAL questionnaire
Time Frame
8 weeks
Title
Carer quality of life
Description
Measured by CQOLC questionnaire
Time Frame
8 weeks
Title
Change in physical function
Description
Mean daily step count, measured by Physical Activity Meter over 5 days
Time Frame
8 weeks
Title
Change in physical function
Description
Measured by two-minute walk test (metres/feet covered)
Time Frame
8 weeks
Title
Change in physical function
Description
Measured by Karnofsky performance status (KPS) at baseline, mid and endpoint
Time Frame
8 weeks
Title
Change in physical function
Description
Measured by timed up-and-go test (Seconds)
Time Frame
8 weeks
Title
Change in physical function
Description
Measured by Life Space Assessment scores
Time Frame
8 weeks
Title
Sleep quality
Description
Measured by physical activity meter at baseline and endpoint (Mean sleep hours, mean hours restless and hours awake)
Time Frame
8 weeks
Title
Nutritional status
Description
Height and weight measured at baseline, mid and endpoint assessment (m, Kg and combined as kg/m2)
Time Frame
8 weeks
Title
Nutritional status
Description
Measured by PG-SGA nutritional assessment (PG-SGA point score)
Time Frame
8 weeks
Title
Contamination in the control group
Description
Measured by dietary intake using 24 hour recall (patient diary entries)
Time Frame
8 weeks
Title
Contamination in the control group
Description
Measured by change in measures of physical function (see outcomes 4-8) in control group from baseline measurement to endpoint
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Diagnosis of advanced cancer (defined as metastatic or locally advanced cancer not amenable to curative treatment).
Outpatient
≥18years
Karnofsky score ≥ 60
Prognosis greater than 3 months
Able to complete trial based assessments
Under care of community services at Marie Curie or St Columba's Hospices
Ability to comply with trial protocol
Ability to provide and have capacity to consent
Agree to attend trial centre for trial related activity (St Columba's Hospice)
Exclusion Criteria:
Undergoing anti-cancer therapy (hormonal treatment or bisphosphonates permitted)
Using enteral nutrition (NG or similar) or parenteral nutrition
Co-enrolment in drug trials
Inability to swallow
Facility Information:
Facility Name
University of Edinburgh
City
Edinburgh
ZIP/Postal Code
EH4 2XR
Country
United Kingdom
12. IPD Sharing Statement
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Exercise and Nutritional Rehabilitation in Patients With Cancer
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